A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2119n209



Internal ID22828194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42944544..42949253hg38UCSC Ensembl
chr9:44021866..44026575hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384710
hg194710
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5860732, nsv5852969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2119n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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